OMOP Concept 44786699
Genetic diseases history panel Family member HL7.VMR-CDS
StandardObservationLOINC74042-3Clinical Observation
Maps from
0
Descendants
5
Valid from
26 Dec 2013
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Synonyms
Alternative names recorded for Genetic diseases history panel Family member HL7.VMR-CDS across source vocabularies.
- CLIN; Diseases Hx Pnl; Fam Mem; Genetic diseases hx Pnl; Genetics; Genomic; Hx; Pan; PANEL.CLINICAL; Panl; Pnl; Point in time; Random
- Genetic diseases hx Pnl Fam Mem VMR-CDS
- 遗传性疾病史组套:-:时间点:^家庭成员:-:HL7.VMR-CDS
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(8)Roll up to these when you need a wider cohort.
- 1Clinical NEC (not elsewhere classified) set
- 1Genetic diseases history panel | Family member | Clinical panels
- 1Virtual Medical Record for Clinical Decision Support panel HL7.VMR-CDS
- 2Clinical panels
- 2Order set
- 2Virtual Medical Record for Clinical Decision Support panel | Patient | Clinical panels
- 3Clinical
- 4{component}
Narrower concepts
(5)Included automatically when you query with descendants.
Get this concept via the API
Resolve Genetic diseases history panel Family member HL7.VMR-CDS - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/44786699?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card